FDA Letter API

13th Floor Elevapors LLC - s

Letter data

Company
13th Floor Elevapors LLC - s
Recipient
13th Floor Elevapors LLC - s | United States
Issue date
2018-07-31
Posted date
Not available
FDA office
United States
Subject
Not available
Product
Tobacco
CMS ID
Not available
Reference number
Not available
FEI
Not available
Inspection dates
2018-06-14 to 2018-07-19

Normalized citations

21 CFR: None found

21 U.S.C.: None found

Related FDA links

No related FDA letter link is present in the source index.

Full source text

CLOSEOUT LETTER 13th Floor Elevapors LLC - s July 31, 2018 More Warning Letters Warning Letters About Warning and Close-Out Letters Product: Tobacco Recipient: 13th Floor Elevapors LLC - s United States Issuing Office: United States Center for Tobacco Products 10903 New Hampshire Avenue Silver Spring, MD 20993 July 31, 2018 VIA UPS and Electronic Mail Chris Warkenton and Randall Dalby 13th Floor Elevapors, LLC 3303 Harbor Blvd Suite F5 Costa Mesa, CA 92626 chris@elevapors.com randy@elevapors.com RE: Warning Letter issued to 13th Floor Elevapors, LLC (RW1800861) Dear Chris Warkenton and Randall Dalby: On May 10, 2018, the United States Food and Drug Administration’s (FDA) Center for Tobacco Products (CTP) issued you a Warning Letter informing you that your Frank ‘N Vape e-liquid product is misbranded under section 903(a)(1) and/or 903(a)(7)(A) of the Federal Food, Drug, and Cosmetic Act (FD&C Act) because its labeling and/or advertising is false or misleading . Specifically, FDA determined that the labeling and/or advertising of your Frank ‘N Vape e-liquid is misleading under section 903(a)(1) and/or 903(a)(7)(A) of the FD&C Act because it causes the product to imitate food products, particularly ones that are marketed toward, and/or appealing to, children. On May 26, 2018, May 30, 2018, July 5, 2018, and July 19, 2018, you sent FDA a response to the Warning Letter, and we held teleconferences on June 14, 2018 and July 19, 2018 to discuss the Warning Letter and your response. In response to the Warning Letter, you stated that you implemented corrective actions to address the violations identified in the Warning Letter. Based on our evaluation, it appears that you have taken steps to address the violation identified in the Warning Letter. This letter does not relieve you or your firm from the responsibility of taking all necessary steps to ensure sustained compliance with the FD&C Act and its implementing regulations or with other relevant legal authority. This letter also will not preclude any regulatory action should violations be observed in the future. Should you have any questions or concerns, please contact me at (301) 796-9235 or by email at elenita.ibarrapratt@fda.hhs.gov . Sincerely, /S/ Ele Ibarra-Pratt Division Director Office of Compliance and Enforcement Center for Tobacco Products VIA UPS and Electronic Mail cc: Phil Daman Daman and Associates, LLP 1455 Pennsylvania Ave, Suite 400 Washington, D.C. 20004 Phillip.daman@damanllp.com Domains By Proxy, LLC 13thfloorelevapors.com@domainsbyproxy.com elevapors.com@domainsbyproxy.com GoDaddy.com, Inc. abuse@godaddy.com Content current as of: 08/23/2018 Regulated Product(s) Tobacco